Canonical Allele Identifier: CA388650399

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733963C>G (hg19) ; chr13:g.101081612C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081612C>G , CM000675.2:g.101081612C>G	GRCh38
NC_000013.10:g.101733963C>G , CM000675.1:g.101733963C>G	GRCh37
NC_000013.9:g.100531964C>G	NCBI36
NG_053176.1:g.340595G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3800G>C MANE Select	ENSP00000251127.6:p.Gly1267Ala
ENST00000648359.1:c.3800G>C	ENSP00000497465.1:p.Gly1267Ala
ENST00000675150.1:c.3521G>C	ENSP00000502680.1:p.Gly1174Ala
ENST00000675332.1:c.3887G>C	ENSP00000501955.1:p.Gly1296Ala
ENST00000676315.1:c.3713G>C	ENSP00000501603.1:p.Gly1238Ala
ENST00000251127.10:c.3800G>C	ENSP00000251127.6:p.Gly1267Ala
NM_052867.2:c.3800G>C	NP_443099.1:p.Gly1267Ala
XM_011521067.1:c.3857G>C	XP_011519369.1:p.Gly1286Ala
XM_011521068.1:c.3800G>C	XP_011519370.1:p.Gly1267Ala
XM_011521069.1:c.3770G>C	XP_011519371.1:p.Gly1257Ala
XM_011521070.1:c.3578G>C	XP_011519372.1:p.Gly1193Ala
NM_001350748.1:c.3887G>C	NP_001337677.1:p.Gly1296Ala
NM_001350749.1:c.3800G>C	NP_001337678.1:p.Gly1267Ala
NM_001350750.1:c.3713G>C	NP_001337679.1:p.Gly1238Ala
NM_001350751.1:c.3713G>C	NP_001337680.1:p.Gly1238Ala
NM_052867.3:c.3800G>C	NP_443099.1:p.Gly1267Ala
XM_011521067.2:c.3857G>C	XP_011519369.1:p.Gly1286Ala
XM_011521069.2:c.3770G>C	XP_011519371.1:p.Gly1257Ala
XM_017020536.2:c.3353G>C	XP_016876025.1:p.Gly1118Ala
XM_017020537.1:c.3035G>C	XP_016876026.1:p.Gly1012Ala
XM_024449336.1:c.3944G>C	XP_024305104.1:p.Gly1315Ala
NM_052867.4:c.3800G>C MANE Select	NP_443099.1:p.Gly1267Ala
NM_001350748.2:c.3887G>C	NP_001337677.1:p.Gly1296Ala
NM_001350749.2:c.3800G>C	NP_001337678.1:p.Gly1267Ala
NM_001350750.2:c.3713G>C	NP_001337679.1:p.Gly1238Ala
NM_001350751.2:c.3713G>C	NP_001337680.1:p.Gly1238Ala